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Chiral pyrrolidine-azole conjugates: Simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes
Zhang Long2,3; Xu Hui1; Mi XueLing2,3; Luo SanZhong1; Cheng Jin-Pei1,2,3
刊名CHINESE SCIENCE BULLETIN
2010-06-01
卷号55期号:17页码:1735-1741
关键词Pyrrolidine Azole Organocatalysis Michael Addition Nitrostyrene
ISSN号1001-6538
DOI10.1007/s11434-010-3120-9
英文摘要Simple pyrrolidine-azole conjugates have been synthesized and found to be efficient catalysts for asymmetric Michael addition to nitrostyrenes. The identified optimal catalysts, pyrrolidine-azoles 2, 8 and 13, could catalyze the asymmetric Michael addition of a range of Michael donors and nitrostyrenes in high yields (up to 99%) and excellent stereoselectivities (up to 99: 1 dr and 97% ee).
语种英语
出版者SCIENCE PRESS
WOS记录号WOS:000278900800007
内容类型期刊论文
源URL[http://ir.iccas.ac.cn/handle/121111/70129]  
专题中国科学院化学研究所
通讯作者Luo SanZhong
作者单位1.Chinese Acad Sci, BNLMS, CAS Key Lab Mol Recognit & Funct, Inst Chem, Beijing 100190, Peoples R China
2.Nankai Univ, Dept Chem, Tianjin 300071, Peoples R China
3.Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China
推荐引用方式
GB/T 7714
Zhang Long,Xu Hui,Mi XueLing,et al. Chiral pyrrolidine-azole conjugates: Simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes[J]. CHINESE SCIENCE BULLETIN,2010,55(17):1735-1741.
APA Zhang Long,Xu Hui,Mi XueLing,Luo SanZhong,&Cheng Jin-Pei.(2010).Chiral pyrrolidine-azole conjugates: Simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes.CHINESE SCIENCE BULLETIN,55(17),1735-1741.
MLA Zhang Long,et al."Chiral pyrrolidine-azole conjugates: Simple and efficient asymmetric organocatalysts for Michael addition to nitrostyrenes".CHINESE SCIENCE BULLETIN 55.17(2010):1735-1741.
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